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Inorganic Chemistry|June 23, 2022
Two Distinct Cu(II)-V(IV) Superexchange Interactions with Similar Bond Angles in a Triangular "CuV2" FragmentYiran Wang, Masayuki Fukuda, Sergey Nikolaev, et al.Frontiers in Sports and Active Living|June 18, 2025
Parkinson's Elevated: improving healthspanKathleen E McKee, Miriam R Rafferty, Theadora W Sakata, et al.American Journal of Medical Genetics. Part A|June 15, 2007
Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domainTomoko Makishima, Anne C Madeo, Carmen C Brewer, et al.BMC Medical Genetics|February 11, 2011
Variable expressivity of FGF3 mutations associated with deafness and LAMM syndromeSaima Riazuddin, Zubair M Ahmed, Rashmi S Hegde, et al.European Journal of Human Genetics : EJHG|July 16, 2009
DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3Shahid Yar Khan, Saima Riazuddin, Mohsin Shahzad, et al.The Journal of Clinical Investigation|November 23, 2011
Mechanotransduction in mouse inner ear hair cells requires transmembrane channel-like genesYoshiyuki Kawashima, Gwenaëlle S G Géléoc, Kiyoto Kurima, et al.Journal of Medical Internet Research|December 4, 2025
Oura Ring Behavioral Feedback Intervention for Alcohol Reduction in Young Adults: User Experience Evaluation of a Pilot Randomized TrialFrances J Griffith, Oksana K Ellison, Sahiti Kunchay, et al.Elife|October 11, 2017
Molecular architecture underlying fluid absorption by the developing inner earKeiji Honda, Sung Huhn Kim, Michael C Kelly, et al.Wellcome Open Research|August 4, 2022
Bias from questionnaire invitation and response in COVID-19 research: an example using ALSPACAlba Fernández-Sanlés, Daniel Smith, Gemma L Clayton, et al.Plos Genetics|July 23, 2013
SLC26A4 targeted to the endolymphatic sac rescues hearing and balance in Slc26a4 mutant miceXiangming Li, Joel D Sanneman, Donald G Harbidge, et al.Pageof 68